Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06254638

Effectiveness of a Multicomponent Intervention to Promote Physical Activity Levels During the School Day (MOVESCHOOL)

Study based a multicomponent school-based intervention during the school-day (i.e., Physically active learning, active breaks, and active recess) on Physical Activity, health, educational, and cognition outcomes in adolescents.

Recruiting

Interested in participating?

Request Info

Key information

Age range

11 year–16 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Extremadura

Cáceres, 10003, Spain

Location status: Recruiting

Location contact

David Sánchez-Oliva, PhD

CONTACT

[email protected]

660574338

About this study

MOVESCHOOLS is a quasi-experimental study coordinated by fully qualified researchers in physical activity and sport sciences from two universities [University of Cadiz (UCA) and University of Extremadura (UEX), Spain]. This study is aimed at year 1 to year 3 from Secondary Education students (11-16 years old), belonging to 10 schools in Spain (5 schools in Cadiz and 5 schools in Caceres). The schools will be assigned to a control group (n = 5 schools and 400 students) and an intervention group (n = 5 schools and 400 students). The intervention will last 6 months, and will consist of three components:

  • Inclusion of a physically active classes per week.
  • Development of two daily active breaks of 5 minutes duration.
  • Implementation of daily active recesses.

Before and after the intervention, Physical Activity and sedentary time will be assessed by accelerometry, health-related fitness levels by field tests, body composition parameters by anthropometry, academic performance by school grades, positive health (quality of life and self-perception of health) by questionnaire, and cognitive parameters (executive functions and mathematical fluency) by specific cognition tests. In weeks 8 and 16, Physical Activity and sedentary time will also be evaluated as intermediate measures.

At the end of the intervention the researchers will determine the changes of the main outcome variables. Likewise, the main hypotheses raised will be:

  • Students belonging to the experimental group will improve physical activity and will decrease sedentary time during the school-day when comparing to the students belonging to the control group.
  • Students belonging to the experimental group will result in improved in physical and psychological health markers when comparing to the students belonging to the control group.
  • Students belonging to the experimental group will result in improved academic indicators and cognitive markers when comparing to the students belonging to the control group.
  • Students belonging to the experimental group will improve school climate and motivational variables in academic classes compared to students belonging to the control group.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adolescents in 1st, 2nd and 3rd year of ESO.
  • Adolescents with informed consent signed by the family/guardian.
  • Schools with at least 80 students enrolled in 1st, 2nd and 3rd ESO.
  • Schools belonging to the regions of Cáceres and Cádiz.

Exclusion criteria

  • Adolescents with any physical disability or health condition that may limit physical activity levels.
  • Schools participating in any other physical activity or health promotion program.

Treatment and study plan

Multicomponent school-based intervention.

Behavioral

Physically active learning: this type of intervention is carried out once a week for 1 hour outside the classroom. The teachers of the corresponding subject (with the support of the research team) are in charge of the physically active classes.

Active break: the intervention consists of 2 active pauses per day. The development of each pause is carried out through a specific digital platform in which students follow the instructions of an avatar, who is in charge of guiding the realization of the active break. Each active break takes a total of 4 minutes, in which two sets of 20 seconds of work and 10 seconds of rest of four different exercises are performed.

Active break: The intervention consists of a daily active break, every school day of the week. The design and supervision of each active break will be carried out by the support technician and the teaching staff based on the students' tastes.

Primary outcomes

  1. Physical activity and sedentary time

    Time frame: 6 months

    Physical activity and sedentary time will be measured through accelerometry (Actigraph GT3X+, Inc., Pensacola, FL, USA).

Secondary outcomes

  1. Cardiorespiratory capacity

    Time frame: 6 months

    The 20-metres shuttle run test will be used to assess cardiorespiratory fitness. Participants will run the 20-metre distance to the rhythm of a recording. The initial speed is 8.5 km/h and will be increased by 0.5 km/h per section. The race will end when the participant stops due to fatigue or when he/she fails to cross the marked lines to the rhythm of the acoustic signals on two consecutive occasions. The last stage or half stage completed by the competitor will be scored.

  2. Musculoskeletal capacity of upper body

    Time frame: 6 months

    The hand grip test will be used to assess musculoskeletal capacity of upper body. The test shall be performed twice with each hand alternately. The maximum score of each hand in kilograms shall be recorded and the mean value between them shall be calculated.

  3. Musculoskeletal capacity of lower body

    Time frame: 6 months

    Standing broad jump shall be used to assess the musculoskeletal capacity of the lower limbs. The participant shall stand behind a line with feet shoulder width apart. The participant is then asked to jump forward as far as possible with both feet. If he/she rests his/her hands or lifts his/her feet off the ground when landing, the test is invalid. The test shall be performed twice, and the best score recorded in centimetres.

  4. Body mass index

    Time frame: 6 months

    Weight and height will be combined to report BMI in kg/m^2.

  5. Body composition

    Time frame: 6 months

    Waist circumference shall be measured as a body composition variable with a non-elastic tape placed in the frontal plane at the midpoint between the upper iliac spine and the costal border at the mid-axillary line. The measurement shall be taken twice and the mean of the two measurements shall be recorded.

  6. Self-reported screen time

    Time frame: 6 months

    Self-reported screen time will be assessed using the Youth Leisure-time Sedentary Behaviour Questionnaire (YLSBQ). Five questions will be selected from the original questionnaire and participants will be asked to answer them by selecting the amount of time they spend per day on each question, ranging from 0 minutes to 5 or more hours.

  7. Subjective physical fitness

    Time frame: 6 months

    The International Fitness Scale will be used for the assessment of subjective physical fitness. Participants will be asked to rate each of the fitness components on a 5-point Likert-type scale ranging from: "very poor" (1); "poor" (2); "fair" (3); "good" (4) and "very good".

  8. Health status

    Time frame: 6 months

    The EuroQol five dimensions three levels will be used to assessment of health status (EQ-5D-3L).This questionnaire is composed of the dimensions of: (i) mobility; (ii) self-care; (iii) usual activities; (iv) pain/discomfort and (v) anxiety/depression. The three levels that participants should mark a Likert-type scale correspond to (i) no problem; (ii) some problems; (iii) many problem.

  9. Self-perceived health

    Time frame: 6 months

    Self-perceived health will be measured through the classic self-reported health item, where participants will have to classify their health among the following options: "excellent" (5); "very good" (4); "good" (3); "fair" (2) and "poor" (1).

  10. School engagement

    Time frame: 6 months

    The engagement scale (UWES-S-9) will be used to evaluate school engagement. The UWES-S-9 is composed of nine items that reflect the three dimensions of engagement: (i) vigor; (ii) absorption; and (iii) dedication, each dimension is represented by three items that will be evaluated through a Likert-type scale, ranging from "never" (0 points) to "always" (6 points).

  11. Learning perception

    Time frame: 6 months

    Learning perception in mathematics and in general studies will be assessed by means of a questionnaire consisting of eight items. Items 1- 4 will assess the "perceived learning" dimension and items 5-8 will measure the "satisfaction with learning" dimension. All items will be scored according to a five-point Likert scale, where "1" is (strongly disagree) and "5" is (strongly agree).

  12. Academic performance

    Time frame: 6 months

    Academic performance will be evaluated through the marks reported by the schools before and after the intervention.

  13. Inhibition

    Time frame: 6 months

    Inhibition will be evaluated through the Flanker task protocol, part of the NIH Examiner programme. This is a computerised programme where the subject answers the tests individually. The algorithm provided by the program, ranging from 0 to 10, which includes accuracy and reaction time, will be recorded.

  14. Cognitive flexibility

    Time frame: 6 months

    Cognitive flexibility will be evaluated through the Shifting task protocol, part of the NIH Examiner programme. This is a computerised programme where the subject answers the tests individually. The algorithm provided by the program, ranging from 0 to 10, which includes accuracy and reaction time, will be recorded.

  15. Working memory

    Time frame: 6 months

    Working memory will be evaluated through the N-Back protocol, part of the NIH Examiner programme. This is a computerised programme where the subject answers the tests individually. The algorithm provided by the program, ranging from 0 to 10, which includes accuracy and reaction time, will be recorded.

  16. Novelty

    Time frame: 6 months

    Novelty will be assessed through the Novelty Need Satisfaction Scale. Five of the 19 questions that make up the original scale will be selected and participants will be asked to answer them on a Likert-type scale where 1 = "strongly disagree" and 5 = "strongly agree".

  17. School climate

    Time frame: 6 months

    School climate will be assessed using the students' perception of school climate scale (PACE-33). Fifteen items will be evaluated. All items will be scored according to a five-point Likert scale, where "1" is (strongly disagree) and "5" is (strongly agree).

  18. Enjoyment and boredom

    Time frame: 6 months

    Enjoyment and boredom will be assessed using the Spanish version of The Sport Satisfaction Instrument. This scale is composed of eight items. Participants will have to rate their degree of agreement with the items referring to fun or boredom on a five-point Likert-type scale, ranging from 1 (strongly disagree) to 5 (strongly agree).

  19. Dietary patterns

    Time frame: 6 months

    Adherence to the Mediterranean diet will be measured using the updated version 2.0 of the KIDMED questionnaire.

  20. Sociodemographic characteristics

    Time frame: 6 months

    Sociodemographic characteristics will be measured through the Spanish-adapted version III of The Family Affluence Scale. This scale is composed of six questions . Each question is scored on a categorical scale, and the sum of the scores from the six items result in an aggregate index ranging from 0 to 13.

  21. Teachers' perceptions about the feasibility of the intervention program.

    Time frame: 6 months

    Perception about the suitability and the development of the intervention program (perceptions, barriers, points to improve, strengths...) a semi-structured interview will be conducted with the teachers involved in the intervention.

  22. Students' perceptions about the feasibility of the intervention program.

    Time frame: 6 months

    A discussion group will be developed for each of the proposed interventions with a subsample of students, in order to obtain information on the suitability and development of the intervention programme (perceptions, barriers, areas for improvement, strengths, etc.).

Study contacts

Contact information is provided by the study sponsor or research team.

Alberto Grao Cruces, PhD

CONTACT

[email protected]

+34 956 016768

David Sánchez Oliva, PhD

CONTACT

[email protected]

660574338

Sponsors and collaborators

Lead sponsor

University of Extremadura

Other

Collaborators

  • Ministry of Science and Innovation, Spain

Registry information

Acronym: MOVESCHOOL

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Feb 12, 2024
Registry last updated
Sep 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.